POST-DISCHARGE PLASMA COATING DEVICE FOR WIRED SUBSTRATES

Abstract

A post-discharge plasma coating device for a wired substrate comprising an inner tubular electrode on an inner tubular wall for receiving the substrate and a precursor moving axially in a working direction; an outer tubular electrode coaxial with, and surrounding, the inner tubular electrode. The inner and outer electrodes are configured to be supplied with an electrical power source for producing a plasma when a plasma gas is supplied between the electrodes and is thereby excited, the plasma excited gas flowing axially in the working direction and reacting with the precursor in a coating area at the end of the inner tubular wall in the direction. The inner tubular wall extends axially towards the coating area at least until, in various instances beyond, the end of the outer electrode, in the working direction and at least one dielectric tubular wall extends axially between the inner tubular electrode and the outer tubular electrode.

Claims

1.-19. (canceled)

20. A post-discharge plasma coating device for a wired substrate, said device comprising: an inner tubular electrode on an inner tubular wall for receiving a substrate and a precursor moving axially in a working direction; and an outer tubular electrode coaxial with, and surrounding, the inner electrode; wherein the inner and outer electrodes are configured to be supplied with an electrical power source for producing a plasma when a plasma gas is supplied between the electrodes and is thereby excited, the plasma excited gas flowing axially in the working direction and reacting with the precursor in a coating area at the end of the inner tubular wall in the working direction; and wherein the inner tubular electrode extends axially towards the coating area at least until the end of the outer electrode in the working direction and in that at least one dielectric tubular wall extends axially between the inner electrode and the outer electrode.

21. The post-discharge plasma coating device according to claim 20, wherein the inner tubular electrode extends axially towards the coating area beyond the end of the outer electrode in the working direction.

22. The post-discharge plasma coating device according to claim 20, wherein the coating area is such that the plasma excited gas can contact directly the substrate.

23. The post-discharge plasma coating device according to claim 20, wherein the coating area is directly adjacent to the inner tubular wall.

24. The post-discharge plasma coating device according to claim 20, wherein the at least one dielectric tubular wall extends axially beyond the outer electrode in the working direction.

25. The post-discharge plasma coating device according to claim 20, wherein the inner tubular electrode surrounds the inner tubular wall or is formed by the inner tubular wall.

26. The post-discharge plasma coating device according to claim 20, wherein the inner tubular electrode extends axially along a portion of the inner tubular wall, the portion being up to 100%.

27. The post-discharge plasma coating device according to claim 20, wherein the dielectric tubular wall or one of the at least one dielectric tubular wall supports the outer electrode.

28. The post-discharge plasma coating device according to claim 27, wherein the outer electrode extends axially along a portion of the dielectric tubular wall, the portion being at least 10% and up to 100%.

29. The post-discharge plasma coating device according to claim 20, wherein the at least one dielectric tubular wall is made of a dielectric material including but not limited to material taken from the following list: quartz, alumina, silicon dioxide, glass, and any combination thereof.

30. The post-discharge plasma coating device according to claim 27, wherein the dielectric tubular wall supporting the outer electrode is a first dielectric tubular wall, the device comprising a second dielectric tubular wall extending between the inner tubular electrode and the first dielectric tubular wall.

31. The post-discharge plasma coating device according to claim 30, wherein an annular space is provided between the dielectric tubular wall supporting the outer electrode and the inner tubular electrode or between the first and the second dielectric tubular walls, the device comprising a connector configured for supplying the space with the plasma gas for producing the plasma, the connector being axially located opposite to the coating area.

32. The post-discharge plasma coating device according to claim 20, wherein the inner tubular wall is movable axially relative to the rest of the device so as to axially displace the coating area.

33. The post-discharge plasma coating device according to claim 20, further comprising the electrical power source configured for supplying a pulsed or alternating high voltage, the device being configured so that the inner electrode is to be electrically grounded and the outer electrode electrically supplied with the high-voltage.

34. The post-discharge plasma coating device according to claim 33, wherein at least one of the high-voltage of the electrical power source is comprised between 1 and 50 kV and the current supplied by the source to the electrode is less than 1000 mA.

35. The post-discharge plasma coating device according to claim 20, further comprising a confinement tube surrounding the coating area.

36. A method for a continuous coating of a wired substrate with a post-discharge plasma coating device comprising an inner tubular electrode on an inner tubular wall for receiving a substrate and a precursor moving axially in a working direction; and an outer tubular electrode coaxial with, and surrounding, the inner electrode, said method comprising: moving the substrate and a precursor in a working direction through the inner tubular electrode while supplying the outer and inner electrodes to a high-voltage; and supplying a plasma gas between the electrodes, so as to produce a plasma excited gas that flows axially towards a coating area where the plasma excited gas chemically reacts with the precursor on the substrate.

37. The method according to claim 36, wherein the precursor is injected in a liquid or in a gaseous phase with a carrier gas.

38. The method according to claim 37, wherein the mixture of the precursor and the carrier gas is moving through the inner tubular wall at a gas speed inferior, equal or superior to the gas speed of the plasma gas and plasma excited gas.

39. The method according to claim 36, wherein the substrate is dipped or sprayed or impregnated with the precursor before moving through the inner electrode.

Description

DRAWINGS

[0030] FIG. 1 is a schematic representation of the post-discharge plasma coating device in accordance with various embodiments of the present invention.

[0031] FIG. 2 is a longitudinal sectional view of the post-discharge plasma coating device according to various embodiments of the present invention.

[0032] FIG. 3 is a cross sectional view of the post-discharge plasma coating device according to various embodiments of the present invention.

[0033] FIG. 4 is a FTIR spectrum of coating obtained with HMDSO injection in a N.sub.2 plasma post discharge according to various embodiments of the present invention.

[0034] FIG. 5 is a FTIR spectrum of coating obtained with MMA injection in a N.sub.2 plasma post discharge according to various embodiments of the present invention.

DETAILED DESCRIPTION

[0035] The FIGS. 1 to 3 do not define the precise proportions of the elements.

[0036] With reference to the attached FIGS. 1, 2 and 3, reference 2 shows a post-discharge plasma coating device according to the present invention. The post-discharge plasma coating device 2 has a tubular shape and comprises an inner tubular wall 3 configured to receive a wired substrate 4 to be coated. The wired substrate 4 can move axially through the inner tubular wall 3 in a working direction 30 in order to be coated in a coating area 16 represented here in dotted lines. The coating area 16 is adjacent to the inner tubular wall 3 and is such that a plasma excited gas 19 can contact directly the substrate 4. The plasma excited gas 19 (i.e., plasma gas that passes through the plasma zone of the device and that has been activated by energetic species from the plasma) flows axially in the working direction 30 and reacts with a precursor 8 in the coating area 16. The precursor 8 is in various instances in the form of a precursor gas flow. The coating occurs in the coating area 16 where the substrate 4, the plasma excited gas 19 and the precursor 8 mix.

[0037] The inner tubular wall 3 is designed to separate the plasma excited gas 19 and the precursor gas flow 8, as well as to protect the substrate 4 from direct plasma interaction. The inner tubular wall 3 is made of non-porous material. The inner tubular wall 3 is directly surrounded by an inner tubular electrode 6, made of conductive material as shown in FIGS. 2 and 3. However, in various embodiments, the inner tubular wall 3 can form the inner electrode 6. For that, the inner tubular wall 3 could be made of electrical conductive material or a combination of electrical conductive material and dielectric material.

[0038] The inner tubular electrode 6 is surrounded by a coaxial outer tubular electrode 10. The two electrodes 6 and 10 are configured to be supplied with an electrical power source in order to produce a plasma when a plasma gas 12 is supplied between them, the plasma gas being thereby excited. The inner tubular electrode 6 extends axially towards the coating area 16 at least until, in various instances beyond, an end of the outer electrode 10. The end of the outer electrode is in the working direction 30. The plasma excited gas 19 appears at the end of the outer electrode 10, in the working direction 30. The coating area 16 corresponds to an area where the plasma excited gas 19, the substrate 4 and the precursor 8 mix.

[0039] The inner tubular wall 3 is movable axially relative to the rest of the device 2 so as to axially displace the coating area 16.

[0040] The device further comprises at least one dielectric tubular wall 14 extending axially between the two electrodes 6 and 10. This electrode composition, so called dielectric barrier (DBD) discharges avoids the formation of electric arcs and allows the production of a homogenous low energy density plasma. As an exemplary embodiment, a dielectric tubular wall 14 extends axially between the two electrodes 6 and 10 and supports the outer electrode 10. The outer electrode 10 extends axially along a portion of the dielectric tubular wall 14, in various instances at least 10% and up to 100% of the length of the dielectric tubular wall. Optionally, a second dielectric tubular wall (not represented), on and around the inner tubular electrode 6 can be used to form a DBD discharge with a symmetric configuration with two dielectrics.

[0041] The dielectric tubular walls are made of a dielectric material including but not limited to material taken from the following list: quartz, alumina, silicon dioxide, glass, and any combination thereof.

[0042] An annular space 15 or passage (represented in FIG. 3) is provided between the inner tubular electrode 6 and the dielectric tubular wall 14 supporting the outer tubular electrode 10, in order to receive the gas to be ionised. The annular space 15 can have approximately a width of 0.5 to 5 mm. The device 2 also comprises a connector 20 configured for supplying the annular space 15 with the plasma gas 12 for producing the plasma. The connector 20 (represented in FIG. 1) is axially located opposite to the coating area 16. In the case of a second dielectric tubular wall, the annular space can be between the dielectric tubular supporting the outer electrode, the dielectric tubular wall being a first dielectric tubular wall, and the second dielectric tubular wall.

[0043] The device 2 further comprises an electrical power source 18 (represented in FIG. 1) configured for supplying a pulsed or alternating high voltage in order to ionize the plasma gas 12 flowing through the annular space 15. The electrical power source 18 is further configured so that the inner electrode 6 is electrically grounded and the outer electrode 10 is electrically supplied with the high voltage. The high voltage of the electrical power source 18 is in various instances comprised between 1 and 50 kV, for example between 1 and 15 kV and/or the current supplied by the power source to the electrode 10 is less than 1000 mA. The frequency of the power source is comprised between 1 kHz and 100 kHz. In general, the power source 18 will produce a high voltage with a low frequency in order to create the plasma. In this manner, when a high voltage is applied to the outer electrode 10, the plasma is created by the phenomenon known as dielectric barrier discharge. A plasma is thus created in between the inner tubular electrode 6 and the dielectric tubular wall 14 supporting the outer electrode. The plasma excited gas 19 will flow axially towards the coating area 16 where the plasma excited gas 19 chemically reacts with the precursor 8 and the substrate 4.

[0044] In order to improve the homogeneity of the coating, the precursor 8 is injected coaxially with the substrate 4 in the inner tubular wall 3. The precursor is in various instances an organic chemical precursor possibly comprising non-organic groups (composed of atoms including but not limited to the list below: Si, Ti, Zr, Zn, Co, Fe, Pt, Pd, S, B, Cl, P, Mg, Ca, Au, Ag), with grow functional interfaces, which allows a good adhesion to the surface of the substrate and exhibits chemical groups of interest. The precursor 8 can be injected in the inner tubular wall 3 in a liquid or gaseous phase, in various instances with a carrier gas. The precursor is in various instances composed of C and H and may include functional groups, such as alcohol, alkane, allyl, amide, amine, carboxylic, epoxyde, etc. and/or unsaturations. The precursor can be for example hexamethyldisiloxane, methyl methacrylate, titanium tetraisopropoxyde, aminopropyltriethoxysilane, the compounds carried in gas comprising but not limited to argon, helium, nitrogen, oxygen, hydrogen, and any combination thereof. In order to prevent the damages induced by high energy species of the plasma (i.e. electrons, ions), the precursor is injected in the inner tubular wall 3 at whatever flow speed, along with a carrier gas flow. The mixture composed of precursor 8 and carrier gas is injected at a gas speed inferior, equal or superior, in various instances equal or superior to the gas speed of the plasma gas 12 and plasma excited gas 19. Alternatively, the substrate 4 can be previously dipped or sprayed or impregnated with the precursor before moving through the inner tubular wall 3.

[0045] Optionally, an external confinement tube (not represented) can be setup in the coating area 16 in order to confine in a limited volume the mixture of the plasma excited gas 19, the chemical precursor 8 and the substrate 4. The confinement tube is in various instances at the end of the outer tubular wall 14.

[0046] The post-discharge plasma coating device 2 can have for example a dielectric tubular wall 14 supporting the outer electrode made of glass with an inner diameter of 10 mm. The outer tubular electrode 10 can have a length of 100 mm and the inner tubular wall 3 can have an outer diameter of 6 mm. The thickness of the inner tubular electrode 6 and outer tubular electrode 10 is comprised between 1 and 1000 m, typically 100-300 m. The annular space 15 between the dielectric tubular wall 14 supporting the outer electrode and the inner tubular electrode can be of 2 mm, the annular space corresponds to the space between the external diameter of the inner tubular electrode and the internal diameter of the dielectric tubular wall supporting the outer electrode.

[0047] Two coatings were performed on metallic wires. A first coating with a monomer of HMDSO (Hexamethyldisiloxane) was performed on a wired substrate made of stainless steel. Nitrogen was used as the plasma gas with a flow speed of 50 l/s. The metallic wire was moved in the device at a speed of 100 cm/min and the HMDSO monomer was injected in the device with a vector gas or carrier gas at a flow speed of 10 l/min. The power supplied by the power source is of 80 W and the frequency of the signal is of 60 kHz. A SiO.sub.2 like coating with very weak SiCH3 absorption bands was observed on the substrate with a Bruker Vertex 70 FTIR spectrometer and the results are represented in FIG. 4.

[0048] A second coating was performed with a monomer of methyl methacrylate (MMA) on a wired substrate made of stainless steel. Nitrogen was used as the plasma gas with a flow speed of 50 l/s. The metallic wire was moved in the device at a speed of 100 cm/min and the methyl methacrylate monomer was injected at a flow of 50 l/min in the device with a carrier gas at a flow speed of 10 l/min. The power supplied by the power source is of 50 W and the frequency of the signal is of 60 Hz. The coating was analysed with the Bruker Vertex 70 FTIR spectrometer and the results are represented in FIG. 5. An organic coating with functional groups CO was observed which revealed that the coating occurred. The monomers used are taken as examples and are not limited.